US2313117A - Chemical product and process of producing same - Google Patents
Chemical product and process of producing same Download PDFInfo
- Publication number
- US2313117A US2313117A US289785A US28978539A US2313117A US 2313117 A US2313117 A US 2313117A US 289785 A US289785 A US 289785A US 28978539 A US28978539 A US 28978539A US 2313117 A US2313117 A US 2313117A
- Authority
- US
- United States
- Prior art keywords
- boiling
- fractions
- fraction
- fuel
- gasoline
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 7
- 239000000126 substance Substances 0.000 title description 2
- 239000000446 fuel Substances 0.000 description 21
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 21
- 238000009835 boiling Methods 0.000 description 20
- 239000003921 oil Substances 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000002407 reforming Methods 0.000 description 6
- 238000005336 cracking Methods 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000001833 catalytic reforming Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G35/00—Reforming naphtha
- C10G35/04—Catalytic reforming
Definitions
- the present invention relates to improvements in the manufacture of moter fuel.
- Boiling A 8. Boiling A. 8.
- M. range T. M. F. Octane F. octane Raf in of individual [meons- Z, Elli-2m 76 99-216 76 208-257 79 200-266 60 248-304 91 255-3)) 49 302-344 60 304-356, 80 354-412 25 343-409 00 7 giving the poorer road performance, whereas fuel A (having the lower octane rating in this range) gives the better read performance.
- the octane rating therefore, eitherin the mid-boiling fraction or in the total light'fraction (up to 325 F.) is directly related "to the road performance.
- the present invention includes preferably reforming the fraction of the motor fuel boiling below about 325 F. catalytically and in the presence of hydrogen. Since the very low boiling fractions from a cracking operation are produced at a relatively high octanelevel, the hydrocarbons boiling approximately up to 200 F. and also thoseboiling from about 325 F. to the end point need not be reformed. Naphthas, however, distilled directly from crude petroleum 011 up to distillation temperatures of about 325 F. must be reformed for best results.
- the 200 F. to 325 F. fraction from some cracking source or the 0 to 325 F. fraction from crude oil are subjected to reforming in the presence of a catalyst, such as alumina admixed with g purely illustrative and do not impose any limi tation on the invention.
- a catalyst such as alumina admixed with g purely illustrative and do not impose any limi tation on the invention.
- Example 1 A naphtha cut obtained directly by distillation from an East Texas crude and which had an end point of about 325 1". was subjected to 9.
- Example 2 An East Texas crude was topped to remove fractions boiling up to about 410 F. A gas oil cut boiling from 470 F. to 800 F. was subjecteda mixture of oxides containing 70% aluminaand M00; at a temperature of 950 F. and a pressure of 300 pounds per square inch at a feed rate of 1 volume of cold oil per volume of catalyst per'hour, the amount of hydrogen present being molar percent of hydrogen based on the average molecular weight of the oil.
- pressures from 50 pounds per square inch to 400 pounds per square inch gauge may be employed while temperatures within the range of from about 925 F. to 1000 F. may be used, and the rate at which the naphtha is fed to the catalyst zone may vary within the range of from 0.5 to 2 volumes of cold oil per volume of catalyst per hour.
- the range of hydrogen concentration employed in this process may vary from 30 to 85 molal percent hydrogen with respect to the average molecular weight of the oil. 01 course,
- the intermediate-or light and intermediate fractions reformed according to the previous examples are blended with relatively heavier'and lighter fractions to producea motor fuel.
- the product produced according to Example 1 maybe blended with heavier and lighter fractions to give a final product in which 17% to 21% is boiled ,off'by heating thelblend to 158 F., 40% boils off at 212 R, -67% boils oil at 257 F., boils oil at 356 1".rand the final end point is about 405 1".
- This motor fuel' would normally be for springor fall use, the winter grades would be more volatile, while the summer would be less volatile.
- the present invention proposes to improve a fuel such as gasoline by reforming the fraction boiling from 0 to 325 F. where this fraction is-not a cracked stock but is virgin naphtha, or by reforming the fraction boiling from 200 F. to 325 F. where the gasoline or this fraction thereof is produced in a cracking operation.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
' Patented Mar. 9, 1943 T o-FFICE CHEMICAL PEODUOIAND PROCESS OF j PRODUCING SAME Arman E. Becker, Westfield, N. 1., assign... a Standard Oil Development Company, a corporation of Delaware No Drawing. Application August 12, i939,
Serial No. 289,785
2 Claims.
The present invention relates to improvements in the manufacture of moter fuel.
It is an object of this invention to produce a motor fuel having an improved octane rating as determined in actual road tests as distinguished from laboratory determinations such as the A. S. T. M. octane rating test.
It is a. further object of this invention to produce a motor fuel having an improved octane rating as determined by an actual road test in automobiles which involves reforming the intermediate fractions of cracked stocks boiling within thegasoline range, preferably catalytically and in the presence of hydrogen, and thereafter blending the proper light, the reformed intermediate, and the proper heavy fractions to produce a gasoline of improved octane rating.
It is a further object of this invention to reform a virgin naphtha fraction boiling below about 325 F. in order to improve its octane rating and to blend this naphtha fraction with other relatively heavier hydrocarbons to produce a gasoline having an end point of about 405 F. or thereabouts.
' At the present time, many motor fuels, particularly those containing addition agents, such as tetraethyl lead, are deficient in anti-knock quality in certain fractions, approximately those distilling between 192 F. and 325 F. It has been found that the road performance of a motor fuel is more directly related to the first 80% distilling off the fuel than to octane rating of the fuel as a whole as determined by the standard A. S. T. M.
procedure. In a gasoline base, therefore, having a distillation end point of about'405 F. with about 40% distilling off at 212'F., the fraction boiling between about 192 F. and 325 F., in the case of a cracked gasoline or the entire product distilling below about 325 F., is the fraction whose A. S. T. M. octane number is most directly related to the road octane number of the entire fuel. The following tests have been carried out with two fuels in order to demonstrate this fact:
Fuel A Fuel B A, S. T. M. rating 71.7 71. 7 Road rating-A verage 4 automobiles made i 1 by 4 different manufacturers 78. 3 73. 1 Diilerence 1 6. 6 1. 4
Boiling A. 8. Boiling A. 8.
range, '1. M. range, T. M. F. Octane F. octane Raf in of individual [meons- Z, Elli-2m 76 99-216 76 208-257 79 200-266 60 248-304 91 255-3)) 49 302-344 60 304-356, 80 354-412 25 343-409 00 7 giving the poorer road performance, whereas fuel A (having the lower octane rating in this range) gives the better read performance. The octane rating, therefore, eitherin the mid-boiling fraction or in the total light'fraction (up to 325 F.) is directly related "to the road performance.
In carrying out this invention, therefore, high octane fractions are concentrated in the midboiling range of a: motor fuel, such as gasoline in the case where the gasoline contains cracked products, or the octane rating of the whole portion of the motor fuel boiling .up to 325 F. is elevated in the case where the fuel contains virgin naphtha in this fraction.. v
It is well known that'normal thermal cracking processes when used for producing high octane motor fuel cause an excessive conversion of the higher boiling fractions to normally gaseous products including -a considerable quantity of octane number in the low boiling range which tapers off to a relatively low octane rating in the higher boiling fractions. It is common practice, therefore, to reform or recrack products boiling within the motor gasoline range in order to raise the octane rating of the higher boiling fractions.
This process, however, not only consumes cracking capacity, but leads to a reduction in the yield of motor gasoline due to the formation of'normally gaseous fractions and heavy polymers.
In order to avoid the necessity of increasing the octane rating of motor fuel as a whole, as
well as to avoid. the above-mentioned defects in prior practice, to produce a product which will have-a high octane rating as determined by road tests as distinguished from A. S. T. M.
laboratory tests. the present invention includes preferably reforming the fraction of the motor fuel boiling below about 325 F. catalytically and in the presence of hydrogen. Since the very low boiling fractions from a cracking operation are produced at a relatively high octanelevel, the hydrocarbons boiling approximately up to 200 F. and also thoseboiling from about 325 F. to the end point need not be reformed. Naphthas, however, distilled directly from crude petroleum 011 up to distillation temperatures of about 325 F. must be reformed for best results. The 200 F. to 325 F. fraction from some cracking source or the 0 to 325 F. fraction from crude oil are subjected to reforming in the presence of a catalyst, such as alumina admixed with g purely illustrative and do not impose any limi tation on the invention.
Example 1? A naphtha cut obtained directly by distillation from an East Texas crude and which had an end point of about 325 1". was subjected to 9.
preferred.
catalytic reforming operation in the presence of hydrogen and an alumina catalyst containing about 97% A120; and 3% CH: at a temperature of about 920 F. and under a pressure of 200.
pounds per square inch gauge pressure while feeding the naphtha through thecatalyst bed at a rate of ,6 volume of cold oil per volume of catalyst per hour, the amount of hydrogen being about 60 moial percent. based on the average molecular weight of the oil.
Example 2 An East Texas crude was topped to remove fractions boiling up to about 410 F. A gas oil cut boiling from 470 F. to 800 F. was subjecteda mixture of oxides containing 70% aluminaand M00; at a temperature of 950 F. and a pressure of 300 pounds per square inch at a feed rate of 1 volume of cold oil per volume of catalyst per'hour, the amount of hydrogen present being molar percent of hydrogen based on the average molecular weight of the oil.
In carrying out the present reforming operation, pressures from 50 pounds per square inch to 400 pounds per square inch gauge may be employed while temperatures within the range of from about 925 F. to 1000 F. may be used, and the rate at which the naphtha is fed to the catalyst zone may vary within the range of from 0.5 to 2 volumes of cold oil per volume of catalyst per hour. The range of hydrogen concentration employed in this process may vary from 30 to 85 molal percent hydrogen with respect to the average molecular weight of the oil. 01 course,
hydrogen need not'be employed, but its use is While catalytic reforming in the'presence of hydrogen gives superior results, it is, of course. possible to reform the I intermediate fractions thermally as follows:
a naphtha obtained bydistillation from a.
Muskegon crude petroleumv boiling up to 325 F. was thermally reformed by heating in a coil to a temperature of 700 to 1000? '1". under a gauge pressure of 700 pounds persquare inch, at a feed rate of 15 volumes of cold oil per volume of reaction zone per hour.
The intermediate-or light and intermediate fractions reformed according to the previous examples are blended with relatively heavier'and lighter fractions to producea motor fuel. For example, the product produced according to Example 1 maybe blended with heavier and lighter fractions to give a final product in which 17% to 21% is boiled ,off'by heating thelblend to 158 F., 40% boils off at 212 R, -67% boils oil at 257 F., boils oil at 356 1".rand the final end point is about 405 1". This motor fuel' would normally be for springor fall use, the winter grades would be more volatile, while the summer would be less volatile.
To recapitulate, the present invention proposes to improve a fuel such as gasoline by reforming the fraction boiling from 0 to 325 F. where this fraction is-not a cracked stock but is virgin naphtha, or by reforming the fraction boiling from 200 F. to 325 F. where the gasoline or this fraction thereof is produced in a cracking operation. 1
It is obvious that many modifications of this invention falling within the spirit of the same will readily occur to those skilled in this art.
I claim:
1. The method of improving the road octane rating of a given body of gasoline which comprises separating from said body fractions boil-.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US289785A US2313117A (en) | 1939-08-12 | 1939-08-12 | Chemical product and process of producing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US289785A US2313117A (en) | 1939-08-12 | 1939-08-12 | Chemical product and process of producing same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2313117A true US2313117A (en) | 1943-03-09 |
Family
ID=23113082
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US289785A Expired - Lifetime US2313117A (en) | 1939-08-12 | 1939-08-12 | Chemical product and process of producing same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2313117A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2424997A (en) * | 1942-10-21 | 1947-08-05 | Houdry Process Corp | Production of aviation gasoline |
| US2487466A (en) * | 1945-04-09 | 1949-11-08 | Union Oil Co | Catalytic desulfurization of hydrocarbons |
| US2589523A (en) * | 1948-06-21 | 1952-03-18 | Pure Oil Co | Blending of hydroformer feed stocks |
-
1939
- 1939-08-12 US US289785A patent/US2313117A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2424997A (en) * | 1942-10-21 | 1947-08-05 | Houdry Process Corp | Production of aviation gasoline |
| US2487466A (en) * | 1945-04-09 | 1949-11-08 | Union Oil Co | Catalytic desulfurization of hydrocarbons |
| US2589523A (en) * | 1948-06-21 | 1952-03-18 | Pure Oil Co | Blending of hydroformer feed stocks |
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